JP4649376B2 - Anti-boiled agent - Google Patents
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- JP4649376B2 JP4649376B2 JP2006200955A JP2006200955A JP4649376B2 JP 4649376 B2 JP4649376 B2 JP 4649376B2 JP 2006200955 A JP2006200955 A JP 2006200955A JP 2006200955 A JP2006200955 A JP 2006200955A JP 4649376 B2 JP4649376 B2 JP 4649376B2
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Description
本発明は、煮崩れ防止剤およびその製造方法ならびに煮崩れ防止方法に関する。 The present invention relates to an anti-collapse agent, a production method thereof, and an anti-collapse method.
ジャガイモ、ニンジン、ダイコン等の野菜、白身魚等の魚介類等は、調理において煮込む際に、形状が崩れる、いわゆる煮崩れしやすいことが知られている。
煮崩れを防止する方法としてはアルコールを添加する方法が知られているが、それ以外の方法としては、卵殻中のカルシウム成分を含む酢酸水溶液を加える野菜の煮崩れ防止方法(特許文献1参照)、キトサン溶液を塗布あるいは含浸させる軟組織の野菜、魚介類などの食品素材の煮崩れ防止方法(特許文献2参照)、ニゲロオリゴ糖を0.1〜30重量%含有する溶液中に浸漬する煮崩れの顕著な食品の煮崩れ防止方法(特許文献3参照)等が知られている。しかし、これらの方法では煮崩れ防止効果が不十分であったり、好ましくない風味が付与されたりする問題があった。
It is known that vegetables such as potatoes, carrots and radish, and seafood such as white fish lose their shape when cooked during cooking, so-called boiling.
A method of adding alcohol is known as a method for preventing boiling, but as other methods, a method for preventing vegetable boiling by adding an aqueous acetic acid solution containing a calcium component in eggshell (see Patent Document 1). A method of preventing food materials such as vegetables and seafood from soft tissue to be coated or impregnated with a chitosan solution (see Patent Document 2), and a significant amount of boiling caused by immersion in a solution containing 0.1 to 30% by weight of nigerooligosaccharide A method for preventing food from collapsing (see Patent Document 3) is known. However, these methods have a problem that the effect of preventing boiling is insufficient or an undesirable flavor is imparted.
このため、素材の風味に影響を与えず十分な煮崩れ防止効果を得ることのできる煮崩れ防止剤の開発が望まれている。
本発明の目的は、煮崩れ防止剤、煮崩れ防止剤の製造方法、煮崩れ防止方法、煮崩れの抑えられた飲食品、または該飲食品の製造方法を提供することにある。 An object of the present invention is to provide a boil-in preventing agent, a method for producing a batter-inhibiting agent, a boil-out preventing method, a food or drink with reduced boil-down, or a method for producing the food or drink.
本発明は、以下の(1)〜(7)に関する。
(1) 乳酸菌の菌体を該菌体に損傷を与える処理に供して得られる処理物を有効成分として含有することを特徴とする煮崩れ防止剤。
(2) 乳酸菌の菌体に損傷を与える処理が、有機溶媒処理、超音波処理、界面活性剤処理、酵素処理および機械的破砕処理からなる群より選ばれる処理である、上記(1)の煮崩れ防止剤。
(3) 飲食品素材を煮込む際、上記(1)または(2)の煮崩れ防止剤の存在下で煮込むことを特徴とする、飲食品素材の煮崩れ防止方法。
(4) 上記(1)または(2)の煮崩れ防止剤を添加することを特徴とする、飲食品の製造方法。
(5) 上記(4)の方法により得られる飲食品。
(6) 乳酸菌の菌体を、該菌体に損傷を与える処理に供することを特徴とする煮崩れ防止剤の製造方法。
(7) 乳酸菌の菌体に損傷を与える処理が、有機溶媒処理、超音波処理、界面活性剤処理、酵素処理および機械的破砕処理からなる群より選ばれる処理である、上記(6)の方法。
The present invention relates to the following (1) to (7).
(1) An anti-boil-up agent comprising a treated product obtained by subjecting microbial cells of lactic acid bacteria to a treatment that damages the microbial cells as an active ingredient.
(2) The boil of (1) above, wherein the treatment for damaging lactic acid bacteria is a treatment selected from the group consisting of organic solvent treatment, ultrasonic treatment, surfactant treatment, enzyme treatment and mechanical crushing treatment. Anti-collapse agent.
(3) A method for preventing a food / beverage material from being boiled, wherein the food / beverage material is boiled in the presence of the above-mentioned (1) or (2) boil-out preventing agent.
(4) A method for producing a food or drink, comprising adding the anti-coagulation agent of (1) or (2).
(5) Food / beverage products obtained by the method of said (4).
(6) A method for producing a boil-in preventing agent, wherein the lactic acid bacteria are subjected to a treatment for damaging the bacteria.
(7) The method according to (6) above, wherein the treatment for damaging lactic acid bacteria is a treatment selected from the group consisting of organic solvent treatment, ultrasonic treatment, surfactant treatment, enzyme treatment and mechanical crushing treatment. .
本発明により、煮崩れ防止剤、煮崩れ防止剤の製造方法、飲食品素材の煮崩れ防止方法、素材の煮崩れの抑えられた飲食品、または該飲食品の製造方法を提供することができる。 INDUSTRIAL APPLICABILITY According to the present invention, it is possible to provide an anti-boiled agent, a method for producing an anti-boiled agent, an anti-boiled food material, a food / beverage product in which the material is prevented from being boiled, or a method for producing the food / beverage product. .
本発明の煮崩れ防止剤は、乳酸菌の菌体を、該菌体に損傷を与える処理に供して得られる処理物を含有する組成物であればよく、また、必要に応じて無機塩、酸、アミノ酸、核酸、糖、調味料、香辛料、賦形剤等の飲食品に使用可能な各種添加物、エタノール等のアルコールを含有してもよい。
無機塩としては、塩化ナトリウム、塩化カリウム、塩化カルシウム等があげられる。
酸としては、フマル酸、リンゴ酸、酒石酸、クエン酸、脂肪酸等のカルボン酸等があげられる。
The anti-collapse agent of the present invention may be a composition containing a treated product obtained by subjecting microbial cells to a treatment that damages the microbial cells, and if necessary, an inorganic salt, an acid. , Amino acids, nucleic acids, sugars, seasonings, spices, various additives usable for food and drink such as excipients, and alcohols such as ethanol.
Examples of inorganic salts include sodium chloride, potassium chloride, calcium chloride and the like.
Examples of the acid include carboxylic acids such as fumaric acid, malic acid, tartaric acid, citric acid, and fatty acids.
アミノ酸としては、グルタミン酸ナトリウム、グリシン、アラニン等があげられる。
核酸としては、イノシン酸ナトリウム、グアニル酸ナトリウム等があげられる。
糖としては、ショ糖、ブドウ糖、乳糖等があげられる。
調味料 としては、醤油、味噌、酢、みりん、アルコール含有発酵調味料、畜肉エキス、家禽エキス、魚介エキス、酵母エキス、蛋白質加水分解物等があげられる。
Examples of amino acids include sodium glutamate, glycine, and alanine.
Examples of the nucleic acid include sodium inosinate and sodium guanylate.
Examples of the sugar include sucrose, glucose, and lactose.
Examples of the seasoning include soy sauce, miso, vinegar, mirin, alcohol-containing fermented seasoning, livestock meat extract, poultry extract, seafood extract, yeast extract, protein hydrolyzate, and the like.
香辛料としては、スパイス類、ハーブ類等があげられる。賦形剤としては、デキストリン、各種澱粉等があげられる。
本発明の煮崩れ防止剤は、液状、粉状、顆粒状等のいずれの形状を有するものであってもよい。
本発明の煮崩れ防止剤の調製に用いられる乳酸菌の菌体は、乳酸菌を培地で培養して調製することができる。市販の乳酸菌の菌体を用いてもよい。
Spices include spices and herbs. Examples of the excipient include dextrin and various starches.
The anti-collapse agent of the present invention may have any shape such as liquid, powder or granule.
The bacterial body of lactic acid bacteria used for the preparation of the anti-collapse agent of the present invention can be prepared by culturing lactic acid bacteria in a medium. Commercially available lactic acid bacteria may be used.
乳酸菌としては、ラクトバチルス(Lactobacillus)属、ぺディオコッカス(Pediococcus)属、またはストレプトコッカス(Streptococcus)属に属する乳酸菌があげられる。
ラクトバチルス属に属する微生物としては、ラクトバチルス・プランタラム(Lactobacillus plantarum)、ラクトバチルス・ペントサス(Lactobacillus pentosus)、ラクトバチルス・サケ(Lactobacillus sake)、ラクトバチルス・サンフランシスコ(Lactobacillus sanfrancisco)、ラクトバチルス・フラクチボランス(Lactobacillus fructivorans)、ラクトバチルス・ホモヒオチ(Lactobacillus homohiochii)、ラクトバチルス・ヒルガルディ(Lactobacillus hilgardii)等に属する乳酸菌があげられる。ペディオコッカス属に属する乳酸菌としては、ペディオコッカス・ペントサセウス(Pediococcus pentosaceus)等に属する乳酸菌があげられる。ストレプトコッカス属に属する微生物としては、ストレプトコッカス・サーモフィラス(Streptococcus thermophilus)等に属する乳酸菌があげられる。
The lactic acid bacteria, Lactobacillus (Lactobacillus) genus, Pediococcus (Pediococcus) genus, or lactic acid bacteria belonging to the Streptococcus (Streptococcus) genus, and the like.
As a microorganism belonging to the genus Lactobacillus, Lactobacillus plantarum (Lactobacillus plantarum), Lactobacillus pentosus (Lactobacillus pentosus), Lactobacillus sake (Lactobacillus sake), Lactobacillus San Francisco (Lactobacillus sanfrancisco), Lactobacillus Furakuchiboransu ( Lactobacillus fructivorans ), Lactobacillus homohiochii , Lactobacillus hilgardii, and the like. Examples of lactic acid bacteria belonging to the genus Pediococcus include lactic acid bacteria belonging to Pediococcus pentosaceus and the like. Examples of microorganisms belonging to the genus Streptococcus include lactic acid bacteria belonging to Streptococcus thermophilus and the like.
これらの乳酸菌の中で、ラクトバチルス属に属する乳酸菌が好ましく用いられ、ラクトバチルス・プランタラム、ラクトバチルス・ペントサス、ラクトバチルス・フラクチボランスに属する乳酸菌がさらに好ましく用いられる。
上記乳酸菌は単独で用いてもよいし、複数を組み合わせて用いてもよい。
乳酸菌を培養する培地は、炭素源、窒素源、無機物、微量成分等を含有していれば、合成培地および天然培地のいずれの培地も用いることができる。培地は液体培地および固体培地のいずれであってもよい。
Among these lactic acid bacteria, lactic acid bacteria belonging to the genus Lactobacillus are preferably used, and lactic acid bacteria belonging to Lactobacillus plantarum, Lactobacillus pentosus, Lactobacillus fractivorans are more preferably used.
The above lactic acid bacteria may be used alone or in combination.
As a medium for culturing lactic acid bacteria, any of a synthetic medium and a natural medium can be used as long as it contains a carbon source, a nitrogen source, an inorganic substance, a trace component, and the like. The medium may be either a liquid medium or a solid medium.
炭素源としては、澱粉、デキストリン、シュクロース、グルコース、マンノース、フルクトース、ラフィノース、ラムノース、イノシトール、ラクトース、マルトース、キシロース、アラビノース、マンニトール、糖蜜、ピルビン酸等があげられ、これらを単独または組合せて用いることができる。
窒素源としては、塩化アンモニウム、硫酸アンモニウム、リン酸アンモニウム、炭酸アンモニウム、酢酸アンモニウム等のアンモニウム塩、硝酸ナトリウム、硝酸カリウム等の硝酸塩、ペプトン、酵母エキス、肉エキス、麦芽エキス、コーン・スティープ・リカー、カゼイン分解物、大豆粉、野菜ジュース、カザミノ酸、尿素、等の窒素含有有機物等があげられ、これらを単独または組合せて用いることができる。
Examples of the carbon source include starch, dextrin, sucrose, glucose, mannose, fructose, raffinose, rhamnose, inositol, lactose, maltose, xylose, arabinose, mannitol, molasses, pyruvic acid and the like, and these are used alone or in combination. be able to.
Nitrogen sources include ammonium salts such as ammonium chloride, ammonium sulfate, ammonium phosphate, ammonium carbonate, and ammonium acetate, nitrates such as sodium nitrate and potassium nitrate, peptone, yeast extract, meat extract, malt extract, corn steep liquor, and casein. Decomposed products, soy flour, vegetable juice, casamino acid, urea, and other nitrogen-containing organic substances can be used, and these can be used alone or in combination.
無機物としては、塩化ナトリウム、塩化カリウム、塩化カルシウム、硫酸マグネシウム、炭酸カルシウム、リン酸一水素カリウム、リン酸二水素カリウム、リン酸マグネシウム、リン酸カリウム、硫酸第一鉄、塩化カルシウム、硫酸マンガン、硫酸亜鉛、硫酸銅等があげられ、これらを単独または組合せて用いることができる。
微量成分としては、パントテン酸、ビオチン、サイアミン、ニコチン酸等のビタミン類、β−アラニン、グルタミン酸等のアミノ酸類等があげられ、これらを単独または組合せて用いることができる。
Examples of inorganic substances include sodium chloride, potassium chloride, calcium chloride, magnesium sulfate, calcium carbonate, potassium monohydrogen phosphate, potassium dihydrogen phosphate, magnesium phosphate, potassium phosphate, ferrous sulfate, calcium chloride, manganese sulfate, Examples thereof include zinc sulfate and copper sulfate, and these can be used alone or in combination.
Examples of the trace component include vitamins such as pantothenic acid, biotin, thiamine, and nicotinic acid, and amino acids such as β-alanine and glutamic acid, and these can be used alone or in combination.
培地は、必要に応じて全乳、全粉乳、脱脂粉乳、生クリーム等の乳製品等、小麦粉、ライ麦粉等の穀物粉等を含有していてもよい。
上記乳製品、穀物粉等をそのまま、または必要に応じて水、上記培地成分等を添加し混合して得られる混合物として、これを天然培地として用いてもよい。
培養条件は、用いる乳酸菌の種類により異なるが、通常10〜50℃、好ましくは20〜40℃で、通常6時間〜20日間、好ましくは1〜15日間行う。液体培地の場合は、必要に応じて通気攪拌してもよい。
The medium may contain whole milk, whole milk powder, skimmed milk powder, dairy products such as fresh cream, etc., and cereal powder such as wheat flour and rye flour, if necessary.
You may use the said dairy product, grain flour, etc. as a natural culture medium as it is, or as a mixture obtained by adding and mixing water, the said culture-medium component, etc. as needed.
The culture conditions vary depending on the type of lactic acid bacterium to be used, but are usually 10 to 50 ° C., preferably 20 to 40 ° C., and usually 6 hours to 20 days, preferably 1 to 15 days. In the case of a liquid medium, aeration and agitation may be performed as necessary.
培養中、炭酸ナトリウム、アンモニア、水酸化ナトリウム等を添加してpHを4〜7となるように、調整することが好ましい。
液体培地で培養した場合、培養後得られる培養液をそのまま乳酸菌の菌体に損傷を与える処理に供してもよいが、培養液を、ろ過、遠心分離等の固液分離して得られる菌体を該処理に供してもよい。
During the culture, it is preferable to adjust the pH to 4 to 7 by adding sodium carbonate, ammonia, sodium hydroxide or the like.
When cultivated in a liquid medium, the culture solution obtained after culturing may be used as it is for the treatment of damaging lactic acid bacteria, but the culture is obtained by solid-liquid separation such as filtration and centrifugation. May be subjected to the treatment.
固体培地で培養した場合、固体培地に生育した菌体を固体培地とともにそのまま乳酸菌の菌体に損傷を与える処理に供してもよいし、固体培地から掻き取るなどの方法で集菌したものを該処理に供してもよい。
乳酸菌の菌体に損傷を与える処理としては、例えば、有機溶媒処理、超音波処理、界面活性剤処理、酵素処理、機械的破砕処理等の処理があげられる。
When cultured in a solid medium, the cells grown on the solid medium may be subjected to a treatment for damaging the lactic acid bacteria as it is together with the solid medium, or those collected by a method such as scraping from the solid medium may be used. You may use for a process.
Examples of the treatment for damaging lactic acid bacteria include organic solvent treatment, ultrasonic treatment, surfactant treatment, enzyme treatment, mechanical crushing treatment, and the like.
有機溶媒処理としては、乳酸菌の菌体に有機溶媒を添加する処理があげられる。
有機溶媒としては、飲食品への利用という観点から、エタノールまたはエタノールに水、りん酸緩衝液、クエン酸緩衝液等の緩衝液を添加して得られるエタノール溶液が好ましくあげられる。
エタノールに緩衝液を添加する場合、緩衝液を構成する酸および塩基の濃度が、エタノール溶液中0.001〜1mol/lとなるように添加することが好ましく、0.01〜0.3mol/lとなるように添加することがさらに好ましい。
Examples of the organic solvent treatment include a treatment of adding an organic solvent to lactic acid bacteria.
The organic solvent is preferably an ethanol solution obtained by adding a buffer solution such as water, a phosphate buffer solution or a citrate buffer solution to ethanol or ethanol from the viewpoint of use in foods and drinks.
When adding a buffer to ethanol, it is preferable to add so that the concentration of the acid and base constituting the buffer is 0.001 to 1 mol / l in the ethanol solution, and 0.01 to 0.3 mol / l. More preferably.
エタノール溶液としては、清酒、焼酎等の酒類、みりん等のアルコール含有調味料を用いてもよい。
エタノール溶液のpHはpH2〜pH8が好ましく、pH3.5〜7がさらに好ましい。
エタノール溶液中のエタノール濃度は0.03〜99%が好ましく、5〜99%がさらに好ましい。
As the ethanol solution, alcohol-containing seasonings such as sake such as sake and shochu, and mirin may be used.
The pH of the ethanol solution is preferably pH 2 to pH 8, and more preferably pH 3.5 to 7.
The ethanol concentration in the ethanol solution is preferably 0.03 to 99%, more preferably 5 to 99%.
菌体に添加する有機溶媒の量に特に限定はないが、例えば、乳酸菌の菌体の湿重量1重量部に対して、1〜100,000重量部が好ましく、1〜10,000重量部がより好ましく、10〜1,000重量部がさらに好ましい。
有機溶媒処理する温度、時間等の処理条件は、乳酸菌の菌体の量、有機溶媒の濃度等により異なるが、通常、10〜95℃で、30秒間〜1ヶ月間である。
The amount of the organic solvent added to the microbial cells is not particularly limited. For example, the amount is preferably 1 to 100,000 parts by weight, more preferably 1 to 10,000 parts by weight with respect to 1 part by weight of the wet weight of the lactic acid bacterium. More preferred is -1,000 parts by weight.
The treatment conditions such as temperature and time for treating with an organic solvent vary depending on the amount of lactic acid bacteria and the concentration of the organic solvent, but are usually 10 to 95 ° C. and 30 seconds to 1 month.
超音波処理としては、超音波破砕機を用いる処理があげられる。乳酸菌の菌体は培養液または菌体の懸濁液中に含有されていることが好ましい。超音波破砕は、超音波出力20〜200W、0〜30℃で、10秒間〜1時間処理することが好ましい。
界面活性剤処理としては、乳酸菌の菌体に界面活性剤を添加する処理があげられる。
界面活性剤としては、食品への利用という観点から、グリセリン脂肪酸エステル、プロピレングリコール脂肪酸エステル、ショ糖脂肪酸エステル、ソルビタン脂肪酸エステル、大豆リン脂質等が好ましく用いられる。
Examples of the ultrasonic treatment include a treatment using an ultrasonic crusher. The cells of lactic acid bacteria are preferably contained in a culture solution or a suspension of cells. The ultrasonic crushing is preferably performed at an ultrasonic output of 20 to 200 W and 0 to 30 ° C. for 10 seconds to 1 hour.
Examples of the surfactant treatment include a treatment of adding a surfactant to lactic acid bacteria.
As the surfactant, glycerin fatty acid ester, propylene glycol fatty acid ester, sucrose fatty acid ester, sorbitan fatty acid ester, soybean phospholipid and the like are preferably used from the viewpoint of use in foods.
脂肪酸エステルの脂肪酸は、直鎖または分岐状の飽和または不飽和の脂肪酸のいずれであってもよいが、直鎖脂肪酸が好ましく、直鎖飽和脂肪酸がさらに好ましい。該脂肪酸の炭素数は1〜24が好ましく、6〜20がさらに好ましい。例えばカプロン酸、カプリル酸、カプリン酸、ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン酸、アラキジン酸等があげられる。 The fatty acid of the fatty acid ester may be a linear or branched saturated or unsaturated fatty acid, preferably a linear fatty acid, and more preferably a linear saturated fatty acid. 1-24 are preferable and, as for carbon number of this fatty acid, 6-20 are more preferable. Examples thereof include caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid and the like.
界面活性剤の添加量は、乳酸菌の菌体に添加して得られる組成物中の界面活性剤の濃度が0.1〜50g/lとなる量が好ましく、1〜20g/lとなる量がさらに好ましい。界面活性剤で処理する温度、時間等の処理条件は、乳酸菌の菌体の量等により異なるが、通常、10〜50℃で、1時間〜1ヶ月間である。
酵素処理としては、乳酸菌の菌体に、リゾチーム等の細胞壁溶解酵素を添加して作用させる処理があげられる。酵素処理する条件は、乳酸菌の種類、用いる酵素の種類等によって異なるが、リゾチームの場合、通常20〜40℃で、1時間〜1ヶ月間である。
The amount of the surfactant added is preferably such that the concentration of the surfactant in the composition obtained by adding to the lactic acid bacteria is 0.1 to 50 g / l, more preferably 1 to 20 g / l. . The treatment conditions such as temperature and time for treatment with the surfactant vary depending on the amount of lactic acid bacteria, but are usually 10 to 50 ° C. and 1 hour to 1 month.
Examples of the enzyme treatment include a treatment in which a cell wall lytic enzyme such as lysozyme is added to act on lactic acid bacteria. The enzyme treatment conditions vary depending on the type of lactic acid bacteria, the type of enzyme used, etc., but in the case of lysozyme, it is usually 20 to 40 ° C. and 1 hour to 1 month.
機械的破砕処理としては、攪拌機、高速攪拌機、回転振とう機等を用いる攪拌処理、フレンチプレス、マントンガウリンホモゲナイザー等を用いる圧力処理等があげられる。
撹拌処理する際、乳酸菌の菌体は培養液または菌体の懸濁液中に含有されていることが好ましい。撹拌速度は50〜10,000rpmが好ましく、100〜1,000rpmがさらに好ましい。
上記の乳酸菌の処理は単独で行ってもよいし、組み合わせて行ってもよい。
Examples of the mechanical crushing treatment include stirring treatment using a stirrer, high-speed stirrer, rotary shaker, etc., pressure treatment using a French press, a Manton Gaurin homogenizer, and the like.
When the stirring treatment is performed, the lactic acid bacteria are preferably contained in a culture solution or a suspension of the bacteria. The stirring speed is preferably 50 to 10,000 rpm, more preferably 100 to 1,000 rpm.
The above treatment of lactic acid bacteria may be performed alone or in combination.
乳酸菌の菌体に上記の処理を行って得られる乳酸菌の菌体の処理物は、そのまま本発明の煮崩れ防止剤に用いてもよいが、必要に応じてろ過、遠心分離等の固液分離処理、脱色処理、濃縮処理、乾燥処理等の処理を、単独で、または組み合わせて行って得られる、ろ液、脱色液、濃縮液、乾燥物等を本発明の防止剤に用いてもよい。
本発明の煮崩れ防止方法としては、飲食品素材を煮込む工程を有する飲食品の製造において、飲食品素材を本発明の煮崩れ防止剤の存在下で煮込む以外は該飲食品の通常の製造方法をあげることができる。
The processed product of lactic acid bacteria obtained by subjecting the lactic acid bacteria to the above-mentioned treatment may be used as it is for the anti-boiling agent of the present invention, but if necessary, solid-liquid separation such as filtration, centrifugation, etc. A filtrate, a decolorizing solution, a concentrated solution, a dried product, or the like obtained by performing treatment, decoloration treatment, concentration treatment, drying treatment or the like alone or in combination may be used as the inhibitor of the present invention.
As the method for preventing boil-down of the present invention, in the production of food / beverage products having a step of boiling the food / beverage material, a normal method for producing the food / beverage products, except that the food / beverage material is boiled in the presence of the boil-off preventing agent of the present invention Can give.
飲食品素材としては、煮崩れしやすいものが好ましくあげられる。たとえば、ジャガイモ、サトイモ、サツマイモ等のイモ類、ニンジン、ダイコン、カボチャ等の野菜、ダイズ、インゲン豆等の豆類、サバ、ブリ、タイ、ヒラメ、カレイ、フグ等の魚介類、豚肉、牛肉等の肉類等があげられる。
飲食品素材を煮込む工程を有する飲食品としては、たとえば、肉じゃが、筑前煮、煮しめ、ぶり大根、煮豆、味噌煮、クリーム煮、カレー、シチュー、豚の角煮等があげられる。
As the food / beverage material, a material that is easily boiled is preferable. For example, potatoes such as potatoes, taros and sweet potatoes, vegetables such as carrots, radish and pumpkins, beans such as soybeans and kidney beans, seafood such as mackerel, yellowtail, thailand, flounder, flounder and puffer, pork and beef Examples include meat.
Examples of the food and drink having the step of simmering the food and drink material include meat potato, Chikuzen boiled, boiled, radish, boiled beans, miso boiled, cream boiled, curry, stew, and pork simmered.
飲食品素材を本発明の煮崩れ防止剤の存在下で煮込む方法としては、例えば、本発明の煮崩れ防止剤を、飲食品素材100重量部に対して、0.00001〜20重量部、好ましくは0.00005〜10重量部添加して煮込む方法があげられる。
煮込む温度、時間等の条件は、通常50〜100℃で1分間〜24時間である。
以下に本発明の実施例を示す。
Examples of the method for simmering the food / beverage material in the presence of the anti-collapse agent of the present invention include, for example, 0.00001-20 parts by weight, preferably 0.00005, of the anti-boiled agent of the present invention with respect to 100 parts by weight of the food / beverage material. A method of adding ~ 10 parts by weight and simmering is mentioned.
The conditions such as the boiling temperature and time are usually 50 to 100 ° C. for 1 minute to 24 hours.
Examples of the present invention are shown below.
ラクトバチルス・ペントサス(Lactobacillus pentosus)NBRC12011株を、一般乳酸菌接種用培地「ニッスイ」(日水製薬社製)50mlに植菌し、30℃で2日間静置培養した。
培養後、培養液を3,000rpmで10分間遠心分離して菌体を回収した。
回収した菌体を滅菌水で洗浄した後、菌体1g(湿重量)を、エタノールの含有量10%(v/v)の緩衝液(0.1mol/lのりん酸水素二ナトリウムおよび0.05mol/Lのクエン酸を含有し、pH4.5の緩衝液)100mlに添加して懸濁し、85℃で1分間加熱した。
Lactobacillus pentosus (Lactobacillus pentosus) NBRC12011 shares, general lactic acid bacteria inoculated medium "Nissui" (Nissui Pharmaceutical Co., Ltd.) was inoculated into 50ml, was allowed to stand for 2 days of culture at 30 ℃.
After the culture, the culture was centrifuged at 3,000 rpm for 10 minutes to recover the cells.
After washing the collected cells with sterilized water, 1 g (wet weight) of the cells was added to a 10% (v / v) ethanol buffer solution (0.1 mol / l disodium hydrogenphosphate and 0.05 mol / l). L was added to 100 ml of a buffer (containing 4.5 citric acid and pH 4.5), and the mixture was suspended at 85 ° C. for 1 minute.
加熱処理後、得られた処理物を3,000rpmで10分間遠心分離し、上清を回収してラクトバチルス・ペントサスNBRC12011株の菌体のエタノール処理物(以下、乳酸菌の菌体の処理物という)を得た。
また、菌体を添加しない以外は同様の処理を行ってコントロールを調製した。
乳酸菌の菌体の処理物およびコントロールを肉じゃがの調味液(醤油、砂糖およびみりんを含む)に0.1%(w/w)となるように添加し、常法に準じて肉じゃがを調製した。なお、煮込み時間は30分間である。
After the heat treatment, the obtained treated product is centrifuged at 3,000 rpm for 10 minutes, and the supernatant is recovered and treated with ethanol of Lactobacillus pentosus NBRC12011 strain (hereinafter referred to as a treated product of lactic acid bacteria). Got.
Further, a control was prepared by carrying out the same treatment except that no cells were added.
The processed product of lactic acid bacteria and the control were added to meat potato seasoning (including soy sauce, sugar and mirin) so that the concentration was 0.1% (w / w), and meat potato was prepared according to a conventional method. The cooking time is 30 minutes.
得られた肉じゃが中のジャガイモの外観上の煮崩れの状態について、10名のパネラーにより、2点比較法で評価した。
その結果、10名全員がコントロールの方が煮崩れが激しいとの評価であり、有意差(危険率1%)が認められた。
なお、いずれの肉じゃがにおいても、乳酸菌の菌体による臭いおよび乳酸菌の発酵により生じる独特の風味は感じられなかった。
The boiled state of the potatoes in the meat potatoes obtained was evaluated by 10 panelists using a two-point comparison method.
As a result, all the 10 people evaluated that the control was more severely boiled, and a significant difference (risk rate 1%) was recognized.
In any meat potato, the smell of lactic acid bacteria and the unique flavor produced by fermentation of lactic acid bacteria were not felt.
本発明により、煮崩れ防止剤、煮崩れ防止剤の製造方法、煮崩れ防止方法、煮崩れの抑えられた飲食品、または該飲食品の製造方法を提供することができる。 ADVANTAGE OF THE INVENTION By this invention, the manufacturing method of an anti-boil-down agent, an anti-boil-up agent, the anti-boil-up method, the food-drinks by which the boil-up was suppressed, or the manufacturing method of this food-drinks can be provided.
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